3-Hydroxy-2-nitrobenzenesulfonamide

Base Information

Chemical Name:3-Hydroxy-2-nitrobenzenesulfonamide
CAS No.:855426-17-4
Molecular Formula:C₆H₆N₂O₅S
Molecular Weight:218.19
Hs Code.:
DSSTox Substance ID:DTXSID601292977

Synonyms:3-hydroxy-2-nitrobenzenesulfonamide;855426-17-4;SCHEMBL7534911;DTXSID601292977;GS0880

Suppliers and Price of 3-Hydroxy-2-nitrobenzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 3-Hydroxy-2-nitrobenzenesulfonamide

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:217.99974247
Heavy Atom Count:14
Complexity:316

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=C(C(=C1)S(=O)(=O)N)[N+](=O)[O-])O

Technology Process of 3-Hydroxy-2-nitrobenzenesulfonamide

There total 2 articles about 3-Hydroxy-2-nitrobenzenesulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 20759-40-4
3-hydroxybenzenesulfonamide

: 855426-17-4
3-hydroxy-2-nitro-benzenesulfonic acid amide

Guidance literature:: With sulfuric acid; water; nitric acid;
DOI:10.1039/jr9500001760

Reference yield:

: 98-18-0
m-aminobenzenesulfonamide

: 855426-17-4
3-hydroxy-2-nitro-benzenesulfonic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: NaNO₂; aqueous H₂SO₄ / anschliessendes Erwaermen

2: water; H₂SO₄; HNO₃

With sulfuric acid; water; nitric acid; sodium nitrite;
DOI:10.1039/jr9500001760